Canonical Allele Identifier: CA2584321416

Gene: PEPD

Linked Data

• gnomAD v4: 19-33387297-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.33387298_33387299del , CM000681.2:g.33387298_33387299del	GRCh38
NC_000019.9:g.33878204_33878205del , CM000681.1:g.33878204_33878205del	GRCh37
NC_000019.8:g.38570044_38570045del	NCBI36
NG_013358.1:g.139595_139596del
NG_013358.2:g.139595_139596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588328.7:c.*45_*46del	ENSP00000468516.4:n.*45_*46del
ENST00000651901.2:c.*45_*46del	ENSP00000498922.2:n.*45_*46del
ENST00000698359.1:c.*45_*46del	ENSP00000513682.1:n.*45_*46del
ENST00000698360.1:c.*45_*46del	ENSP00000513683.1:n.*45_*46del
ENST00000698361.1:c.*155_*156del	ENSP00000513684.1:n.*155_*156del
ENST00000698362.1:c.*664_*665del	ENSP00000513685.1:n.*664_*665del
ENST00000698426.1:c.*45_*46del	ENSP00000513713.1:n.*45_*46del
ENST00000698427.1:c.*45_*46del	ENSP00000513714.1:n.*45_*46del
ENST00000698428.1:c.*45_*46del	ENSP00000513715.1:n.*45_*46del
ENST00000698429.1:n.1410_1411del
ENST00000698430.1:c.1777_1778del
ENST00000698431.1:c.1264_1265del	ENSP00000513717.1:n.1264_1265del
ENST00000698432.1:c.1336_1337del
ENST00000244137.12:c.*45_*46del MANE Select	ENSP00000244137.5:n.*45_*46del
ENST00000588328.6:c.1582_1583del
ENST00000651901.1:c.1613_1614del
ENST00000244137.11:c.*45_*46del	ENSP00000244137.5:n.*45_*46del
ENST00000397032.8:c.*45_*46del	ENSP00000380226.3:n.*45_*46del
ENST00000436370.7:c.*45_*46del	ENSP00000391890.2:n.*45_*46del
ENST00000589598.5:n.252_253del
ENST00000591968.1:n.599_600del
ENST00000593085.1:n.1414_1415del
NM_000285.3:c.*45_*46del	NP_000276.2:n.*45_*46del
NM_001166056.1:c.*45_*46del	NP_001159528.1:n.*45_*46del
NM_001166057.1:c.*45_*46del	NP_001159529.1:n.*45_*46del
NM_000285.4:c.*45_*46del MANE Select	NP_000276.2:n.*45_*46del
NM_001166056.2:c.*45_*46del	NP_001159528.1:n.*45_*46del
NM_001166057.2:c.*45_*46del	NP_001159529.1:n.*45_*46del